Double-blind, Randomized, Placebo-controlled, Prospective Phase III Study Evaluating Efficacy and Safety of Panzyga in Primary Infection Prophylaxis in Patients With Chronic Lymphocytic Leukemia ("PRO-SID" Study)

Inclusion Criteria:

1. Treatment-naïve or relapsed/refractory CLL patients undergoing CLL antineoplastictreatment. Diagnosis of B-cell CLL established according to International Workshopon Chronic Lymphocytic Leukemia (iwCLL) criteria and documented within medicalrecords.

2. Hypogammaglobulinemia (IgG levels <5 g/L) as confirmed by the Central Laboratory.

3. ≥18 years of age.

4. Voluntarily given, fully informed written and signed consent obtained before anystudy-related procedures are conducted.

Exclusion Criteria:

1. IgG treatment within 3 months prior to Screening.

2. Antibiotic prophylaxis and/or treatment within 7 days prior to Baseline (with theexception of trimethoprim-sulfamethoxazole [TMP/SMX], diaminodiphenyl sulfone [dapsone] and pentamidine inhalation).

3. Current major infection or >1 major infection in the previous 6 months beforeBaseline.

4. History of anaphylaxis or severe systemic response to immunoglobulin, blood orplasma-derived products or any Panzyga component.

5. History of a non-CLL malignancy or other medical condition with life-expectancy ofless than two years.

6. Severe liver disease, with signs of ascites and/or hepatic encephalopathy.

7. Severe kidney disease (as defined by estimated glomerular filtration rate [eGFR] <30mL/min/1.73 m2).

8. Body weight >140 kg.

9. Eastern Cooperative Oncology Group (ECOG) performance score of >2 (Appendix 1).

10. Female patients of childbearing potential unwilling to use a protocol-requiredmethod of contraception (as per protocol section 7.3.9 b) from the Screening Visitthroughout the study treatment period and for 30 days following the last dose ofstudy drug.

11. Human immunodeficiency virus (HIV) infection at Screening (defined for the study aspositive HIV antibody test).

12. Patients found to be chronic carriers of hepatitis B virus (HBV), defined bypositive surface antigen (HBsAg), positive Hepatitis B core antibodies (HBcAb)and/or low HBV titers, who will not receive targeted antiviral therapy whileundergoing CLL therapy, and patients with active HBV, defined as high HBV titers.

13. Uncontrolled hepatitis C infection at Screening (defined for the study as positivehepatitis virus C [HCV] polymerase chain reaction [PCR]).

14. Pregnant and lactating women.

15. Subjects with a history of thromboembolic events (TEE) such as deep vein thrombosis,pulmonary embolism, myocardial infarction, ischemic stroke, transient ischemicattack, peripheral artery disease (Fontaine IV) within 6 months before Baseline.

16. Planned or ongoing immunosuppressive treatment (other than for CLL orcorticosteroids) or other forbidden medication during the entire study durationafter study enrollment.

17. Participation in another interventional clinical trial that is either blinded orinvolves an investigational (not approved) product within 3 months before Baselineor during the course of the clinical study. Participation in observational clinicaltrials or open-label trials involving an approved product may be permitted afterconsultation with the medical monitor.

18. Known IgA deficiency with antibodies to IgA.

19. Known blood hyperviscosity, or other hypercoagulable states.

20. Patients unable or unwilling to understand or comply with the study protocol.